SnpEff Annotation and Filtration Element

Annotates and filters variations with SnpEff.

Element type: seff

Parameters

ParameterDescriptionDefault valueParameter in Workflow FileType
Output directorySelect an output directory. Custom - specify the output directory in the ‘Custom directory’ parameter. Workflow - internal workflow directory. Input file - the directory of the input file.Input file
out-modestringstring
Input formatSelect the input format of variations.VCFinp-formatstring
Output formatSelect the format of annotated output files.VCFout-formatstring
GenomeSelect the target genome from the list of SnpEff databases. Genome data will be downloaded if it is not found. The list of databases depends on the SnpEff external tool version.Homo sapiensgenomestring
Upstream/downstream lengthUpstream and downstream interval size. Eliminate any upstream and downstream effects by using 0 length.No upstream/downstream interval (0 bases)updown-lengthnumeric
Canonical transcriptsUse only canonical transcripts.Falsecanonboolean
HGVS nomenclatureAnnotate using HGVS nomenclature.Falsehgvsboolean
Annotate loss of functionAnnotate Loss of function (LOF) and Nonsense-mediated decay (NMD).Falselofboolean
Annotate TFBSs motifsAnnotate transcription factor binding site motifs (only available for the latest GRCh37).Falsemotifboolean

Input/Output Ports

The element has 1 input port:

Name in GUI: Variations

Name in Workflow File: in-file

Slots:

Slot In GUISlot in Workflow FileType
Source urlurlstring

And 1 output port:

Name in GUI: Annotated variations

Name in Workflow File: out-file

Slots:

Slot In GUISlot in Workflow FileType
Source urlurlvariation